Ähnlichkeitssuche

18337

C[C@@H]1CN(Cc2ccc(F)cc2)[C@@H](C)CN1C(=O)COc1ccc(Cl)cc1O
Reaction #11711
title compound
Ausbeute 63.3%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)COc1cc(Cl)ccc1OCC(=O)N1C[C@H](C)N(Cc2ccc(F)cc2)C[C@H]1C
Reaction #11712
title compound
Ausbeute 169.8%DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H]1CN(Cc2ccc(F)cc2)[C@@H](C)CN1C(=O)COc1ccc(Cl)cc1OCC(=O)O
Reaction #11713
title compound
Ausbeute 74.8%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #11714
hydrochloride salt
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(C)Oc1cc(Cl)ccc1OCC(=O)N1C[C@H](C)N(Cc2ccc(F)cc2)C[C@H]1C
Reaction #11715
title compound
Ausbeute 85.5%DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H]1CN(Cc2ccc(F)cc2)[C@@H](C)CN1C(=O)COc1ccc(Cl)cc1[N+](=O)[O-]
Reaction #11728
title compound
Ausbeute 92.5%DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H]1CN(Cc2ccc(F)cc2)[C@@H](C)CN1C(=O)COc1ccc(Cl)cc1N
Reaction #11729
title compound
Ausbeute 69.3%DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H]1CN(Cc2ccc(F)cc2)[C@@H](C)CN1C(=O)COc1ccc(Cl)cc1NS(=O)(=O)CC(=O)O
Reaction #11730
(5-Chloro-2-{2-[4-(4-fluoro-benzyl)-(2R,5S)-2,5-dimethyl-piperazin-1-yl]-2-oxo-ethoxy}-phenylsulfamoyl)-acetic acid
DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H]1CN(Cc2ccc(F)cc2)[C@@H](C)CN1C(=O)COc1ccc(Cl)cc1C=O
Reaction #11731
title compound
Ausbeute 84.5%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)CCNCc1cc(Cl)ccc1OCC(=O)N1C[C@H](C)N(Cc2ccc(F)cc2)C[C@H]1C
Reaction #11732
title compound
Ausbeute 38.4%DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H]1CN(Cc2ccc(F)cc2)[C@@H](C)CN1C(=O)COc1ccc(Cl)cc1CN
Reaction #11736
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C(=O)O)S(=O)(=O)NCc1cc(Cl)ccc1OCC(=O)N1C[C@H](C)N(Cc2ccc(F)cc2)C[C@H]1C
Reaction #11737
desired product
DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H]1CN(Cc2ccc(F)cc2)[C@@H](C)CN1C(=O)COc1ccc(Cl)cc1CO
Reaction #11738
title compound
Ausbeute 98.7%DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H]1CN(Cc2ccc(F)cc2)[C@@H](C)CN1C(=O)COc1ccc(Cl)cc1COCC(=O)OC(C)(C)C
Reaction #11739
title compound
Ausbeute 65.4%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #11740
hydrochloride salt
DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)C(OCc1cc(Cl)ccc1OCC(=O)N1C[C@H](C)N(Cc2ccc(F)cc2)C[C@H]1C)S(N)(=O)=O
Reaction #11741
title compound
Ausbeute 36.8%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccccc1S(=O)(=O)NC(=O)OCc1cc(Cl)ccc1OCC(=O)N1C[C@H](C)N(Cc2ccc(F)cc2)C[C@H]1C
Reaction #11742
(2-Methylbenzenesulfonyl)-carbamic acid 5-chloro-2-{2-[4-(4-fluoro-benzyl)-(2R,5S)-2,5-dimethyl-piperazin-1-yl]-2-oxo-ethoxy}-benzyl ester
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)Cc1cc(Cl)ccc1OCC(=O)N1C[C@H](C)N(Cc2ccc(F)cc2)C[C@H]1C
Reaction #11748
title compound
Ausbeute 97.8%DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H]1CN(Cc2ccc(F)cc2)[C@@H](C)CN1C(=O)COc1ccc(Cl)cc1CC(=O)O
Reaction #11749
title compound
Ausbeute 81.8%DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H]1CN(Cc2ccc(F)cc2)[C@@H](C)CN1C(=O)COc1ccc(Cl)cc1CC(=O)NS(C)(=O)=O
Reaction #11750
title compound
Ausbeute 44.9%DOI: 10.6084/m9.figshare.5104873.v1
Seite 1Weiter